Genes | GeDiPNet - Gene Disease Pathway & Associations

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671 to 680 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
671	102060414	C2-AS1	C2 antisense RNA 1	-	Development disorder, Exudative macular degeneration, Geographic atrophy, Age-related macular degeneration, Rheumatoid arthritis, Schizophrenia
672	10207	PATJ	PATJ crumbs cell polarity complex component	Cipp, INADL, InaD-like, hINADL	Ischemic stroke, Prostatic neoplasms, Prostate cancer
673	1021	CDK6	Cyclin dependent kinase 6	MCPH12, PLSTIRE	Agenesis of corpus callosum, Anemia, Atrial fibrillation, Brain stem neoplasms, Carcinoma of the head and neck, Developmental delay, Dwarfism, Giant cell glioblastoma, Glioblastoma, Mental retardation, Ischemic stroke, Lymphoblastic leukemia, Leukemia, Liposarcoma, Lymphoma View all (17 more)
674	10210	TOPORS	TOP1 binding arginine/serine rich protein, E3 ubiquitin ligase	LUN, P53BP3, RP31, TP53BPL	Cataract, Ciliopathies, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Leukemia, Mental retardation, Nystagmus, Obesity, Optic atrophy View all (4 more)
675	10211	FLOT1	Flotillin 1	-	Diabetes mellitus, Lung cancer, Q fever, Schizophrenia
676	10215	OLIG2	Oligodendrocyte transcription factor 2	BHLHB1, OLIGO2, PRKCBP2, RACK17, bHLHe19	Nonorganic psychosis, Psychosis, Schizophrenia
677	10216	PRG4	Proteoglycan 4	CACP, HAPO, JCAP, MSF, SZP	Arthritis, Arthropathy, Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, Congenital finger flexion contractures, Flexion contracture of wrist, Pericarditis, Pleuropericarditis, Synovial hypertrophy
678	10219	KLRG1	Killer cell lectin like receptor G1	2F1, CLEC15A, MAFA, MAFA-2F1, MAFA-L, MAFA-LIKE	Sjogren`s syndrome
679	10221	TRIB1	Tribbles pseudokinase 1	C8FW, GIG-2, GIG2, SKIP1, TRB-1, TRB1	Coronary arteriosclerosis, Coronary artery disease, Lung carcinoma
680	10225	CD96	CD96 molecule	TACTILE	C syndrome, Camptodactyly of fingers, Chronic obstructive pulmonary disease, Clinodactyly, Congenital diaphragmatic hernia, Dislocated radial head, Congenital epicanthus, Congenital omphalocele, Congenital pectus excavatum, Crohn disease, Cryptorchidism, Cutis laxa, Developmental delay, Dwarfism, Female pseudohermaphroditism View all (21 more)

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